Product Recalls in Missouri
Product recalls affecting Missouri — including food, drugs, consumer products, medical devices, and vehicles distributed to Missouri. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,711 recalls have been distributed to Missouri in the last 12 months.
Showing 2721–2740 of 29,298 recalls
Recalled Item: Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp Recalled by...
The Issue: Baxter is aware of several recalls by other manufacturers related to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp Recalled by...
The Issue: Baxter is aware of several recalls by other manufacturers related to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp Recalled by...
The Issue: Baxter is aware of several recalls by other manufacturers related to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp Recalled by...
The Issue: Baxter is aware of several recalls by other manufacturers related to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Irrigation Tubing for KARL STORZ Endomat Select UP210 Recalled by Karl Storz...
The Issue: Due to improper labeling of products. An intended use on the label has not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Iris Scissors Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...
The Issue: Tip protector may fall off within the packaging, resulting in compromised...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: human med Biofill Infiltration Cannula Recalled by HUMAN MED AG Due to The...
The Issue: The cannula tubes do not comply with the specification. The water jet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Essenz HLM (Heart-Lung Machine) Recalled by LivaNova Deutschland GmbH Due to...
The Issue: Heart-Lung Machine GUI touchscreen may go dark for 10-15 seconds,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CorNeat EverPatch Recalled by CORNEAT VISION, LTD. Due to Retroactive; Due...
The Issue: Retroactive; Due to complaints, labeling correction for permanent...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE procedure kits labeled as follows: 1) COMBINED SPINAL AND EPIDURAL...
The Issue: The connectors may not allow catheters to be inserted as intended if the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smaxel Fractional CO2 Laser Recalled by IDS LTD Due to The Smaxel Fractional...
The Issue: The Smaxel Fractional CO2 Laser does not include a Certification label, and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE procedure kits labeled as follows: 1) CONT EPI 20G W/HUSTEAD...
The Issue: The connectors may not allow catheters to be inserted as intended if the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE procedure kits labeled as follows: 1) 20G EPI CATH SINGLE STERILE...
The Issue: The connectors may not allow catheters to be inserted as intended if the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE procedure kits labeled as follows: 1) ECHOSTIM BLOCK SET Recalled by...
The Issue: The connectors may not allow catheters to be inserted as intended if the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE procedure kits labeled as follows: 1) PERIPHERAL CONTINUOUS NERVE BL...
The Issue: The connectors may not allow catheters to be inserted as intended if the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE procedure kits labeled as follows: 1) L&D CONTINUOUS EPIDURAL TRAY...
The Issue: The connectors may not allow catheters to be inserted as intended if the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE procedure kits labeled as follows: 1) NEURAXIAL KIT Recalled by...
The Issue: The connectors may not allow catheters to be inserted as intended if the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE NEXUS 19/20G CATH CONNECTOR Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: The connectors may not allow catheters to be inserted as intended if the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Acrobat-i Vacuum Stabilizer System. Model Number C-OM-10000Z Recalled by...
The Issue: Deviations in the manufacturing process created a compromise in the sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Acrobat SUV Vacuum Stabilizer System Recalled by Maquet Cardiovascular, LLC...
The Issue: Deviations in the manufacturing process created a compromise in the sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.